Abstract
Reactions of a boryl-substituted acyclic silylene with carbon dioxide and monoxide are reported. The former proceeds through oxygen atom abstraction, generating CO (with rearrangement of the putative silanone product through silyl-group transfer). The latter is characterized by reductive coupling of CO to give an ethynediolate fragment, which undergoes formal insertion into the Si−B bond. The net conversion of carbon dioxide with two equivalents of silylene offers a route for the three-electron reduction of CO 2 to [C 2 O 2 ] 2− .
| Original language | English |
|---|---|
| Pages (from-to) | 1808-1812 |
| Number of pages | 5 |
| Journal | Angewandte Chemie - International Edition |
| Volume | 58 |
| Issue number | 6 |
| DOIs | |
| Publication status | Published - 4 Feb 2019 |
| Externally published | Yes |